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rs762080305

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs762080305(A;A)
Make rs762080305(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position189043179
GeneCOL5A2
is asnp
is mentioned by
dbSNPrs762080305
ebirs762080305
HLIrs762080305
Exacrs762080305
Varsomers762080305
Maprs762080305
PheGenIrs762080305
hapmaprs762080305
1000 genomesrs762080305
hgdprs762080305
ensemblrs762080305
gopubmedrs762080305
geneviewrs762080305
scholarrs762080305
googlers762080305
pharmgkbrs762080305
gwascentralrs762080305
openSNPrs762080305
23andMers762080305
23andMe allrs762080305
SNP Nexus

SNPshotrs762080305
SNPdbers762080305
MSV3drs762080305
GWAS Ctlgrs762080305
Max Magnitude0
ClinVar
Risk rs762080305(A;A)
Alt rs762080305(A;A)
Reference rs762080305(G;G)
Significance Probable-Pathogenic
Disease not specified
Variation info
Gene COL5A2
CLNDBN not specified
Reversed 0
HGVS NC_000002.11:g.189907905G>A
CLNSRC
CLNACC RCV000200339.2,